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Items where Author is "Szépfalusi, Noémi"
Group by: Item Type | No Grouping Jump to: Article Number of items: 1. ArticleSzpisjak, László and Salamon, András and Németh, Viola Luca and Szépfalusi, Noémi and Maróti, Zoltán and Kalmár, Tibor and Zimmermann, Aliz and Zádori, Dénes and Klivényi, Péter (2023) Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient. IDEGGYOGYASZATI SZEMLE / CLINICAL NEUROSCIENCE, 76 (1-2). pp. 63-72. ISSN 0019-1442 |
